曲妥珠单抗
乳腺癌
肿瘤科
拷贝数分析
外显子组测序
内科学
癌症
生物
化疗
拷贝数变化
医学
癌症研究
突变
遗传学
基因
基因组
作者
Marla Lipsyc-Sharf,Esha Jain,Laura C. Collins,Shoshana M. Rosenberg,Kathryn J. Ruddy,Rulla M. Tamimi,Lidia Schapira,Steven E. Come,Jeffrey Peppercorn,Virginia F. Borges,Ellen Warner,Craig Snow,Ian E. Krop,Dewey Kim,Jakob Weiß,Jorge Gómez Tejeda Zañudo,Ann H. Partridge,Nikhil Wagle,Adrienne G. Waks
摘要
PURPOSE Erb-B2 receptor tyrosine kinase 2 ( ERBB2)–positive breast cancer (BC) is particularly common in young women. Genomic features of ERBB2-positive tumors before and after chemotherapy and trastuzumab (chemo + H) have not been described in young women and are important for guiding study of therapeutic resistance in this population. METHODS From a large prospective cohort of women age 40 years or younger with BC, we identified patients with ERBB2-positive BC and tumor tissue available before and after chemo + H. Whole-exome sequencing (WES) was performed on each tumor and on germline DNA from blood. Tumor-normal pairs were analyzed for mutations and copy number (CN) changes. RESULTS Twenty-two women had successful WES on samples from at least one time point; 12 of these had paired sequencing results from before and after chemo + H and 10 had successful sequencing from either time point. TP53 was the only significantly recurrently mutated gene in both pre- and post-treatment samples. MYC gene amplification was observed in four post-treatment tumors. Seven of 12 patients with paired samples showed acquired and/or clonally enriched alterations in cancer-related genes. One patient had an increased clonality putative activating mutation in ERBB2. Another patient acquired a clonal hotspot mutation in TP53. Other genomic changes acquired in post-treatment specimens included alterations in NOTCH2, STIL, PIK3CA, and GATA3. There was no significant change in median ERBB2 CN (20.3 v 22.6; Wilcoxon P = .79) between paired samples. CONCLUSION ERBB2-positive BCs in young women displayed substantial genomic evolution after treatment with chemo + H. Approximately half of patients with paired samples demonstrated acquired and/or clonally enriched genomic changes in cancer genes. ERBB2 CN changes were uncommon. We identified several genes warranting exploration as potential mechanisms of resistance to therapy in this population.
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